Variant report

Variant rs66656487
Chromosome Location chr7:122159691-122159692
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:122154000-122160800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr7:122155800-122171000 Weak transcription H9 Cell Line embryonic stem cell
3 chr7:122157200-122161800 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr7:122157200-122162000 Enhancers HUES48 Cell Line embryonic stem cell
5 chr7:122157200-122162200 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr7:122157400-122162200 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr7:122157600-122162000 Enhancers HUES6 Cell Line embryonic stem cell
8 chr7:122157600-122162200 Enhancers HUES64 Cell Line embryonic stem cell
9 chr7:122157800-122160400 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr7:122158600-122159800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr7:122158600-122160400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr7:122158800-122161400 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr7:122159000-122160800 Weak transcription H1 Cell Line embryonic stem cell
14 chr7:122159200-122160800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr7:122159600-122159800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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